[The toxicological characteristics of Gastrofenzin. II. Its subacute oral toxicity].

Problemi na khigienata Pub Date : 1996-01-01
A Mikhaĭlova, G Antov, Zh Khalkova, Kh Zaĭkov, M Tasheva, S Dinoeva
{"title":"[The toxicological characteristics of Gastrofenzin. II. Its subacute oral toxicity].","authors":"A Mikhaĭlova,&nbsp;G Antov,&nbsp;Zh Khalkova,&nbsp;Kh Zaĭkov,&nbsp;M Tasheva,&nbsp;S Dinoeva","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The subacute (30 day) oral toxicity of Gastrofenzin has been investigated in white rats \"Wistar\" of both sexes, treated with 0.7 and 33 mg.kg-1 for the male and 0.9 and 44 mg.kg-1 for the female rats. The applied doses respond respectively to the control doses, 1/100 and 1/20 LD50 of the preparation. A complex of integral, behaviour, laboratory biochemical and histological methods has been used. The findings show that Gastrofenzin in doses 1/100 and 1/20 LD50 does not exert cumulative effect, reported by the lack of lethal effect among the animals. With the help of actograph \"AIDA\" an increased spontaneous activity is reported in the rats from both sexes treated with dose 1/20 LD50 of the preparation. Under the experimental conditions the doses of 7 and 9 mg.kg-1 (1/100 LD50) and 33 and 44 mg.kg-1 (1/20 LD50) do not exert toxic effect on the liver, kidneys and brain. Deviations are observed which show increasing of the oxidative-metabolic processes and trigger adaptation mechanisms in the above mentioned organs.</p>","PeriodicalId":20520,"journal":{"name":"Problemi na khigienata","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Problemi na khigienata","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The subacute (30 day) oral toxicity of Gastrofenzin has been investigated in white rats "Wistar" of both sexes, treated with 0.7 and 33 mg.kg-1 for the male and 0.9 and 44 mg.kg-1 for the female rats. The applied doses respond respectively to the control doses, 1/100 and 1/20 LD50 of the preparation. A complex of integral, behaviour, laboratory biochemical and histological methods has been used. The findings show that Gastrofenzin in doses 1/100 and 1/20 LD50 does not exert cumulative effect, reported by the lack of lethal effect among the animals. With the help of actograph "AIDA" an increased spontaneous activity is reported in the rats from both sexes treated with dose 1/20 LD50 of the preparation. Under the experimental conditions the doses of 7 and 9 mg.kg-1 (1/100 LD50) and 33 and 44 mg.kg-1 (1/20 LD50) do not exert toxic effect on the liver, kidneys and brain. Deviations are observed which show increasing of the oxidative-metabolic processes and trigger adaptation mechanisms in the above mentioned organs.

胃芬津的毒理学特征。2其亚急性口服毒性]。
本研究对两性大鼠Wistar分别给予0.7 mg和33 mg胃芬津的亚急性(30天)口服毒性进行了研究。男性为1公斤0.9毫克和44毫克。Kg-1为雌性大鼠。所施加剂量分别响应于制剂的对照剂量、1/100和1/20 LD50。一个复杂的积分,行为,实验室生化和组织学的方法已经使用。结果表明,剂量为1/100和1/20 LD50的天麻津不产生累积效应,在动物中没有致死效应。据报道,在“AIDA”的帮助下,在1/20 LD50剂量的大鼠中,两性的自发活性增加。在实验条件下,剂量为7和9mg。kg-1 (1/100 LD50)、33和44 mg。kg-1 (1/20 LD50)对肝、肾、脑无毒性作用。在上述器官中观察到的偏差表明氧化代谢过程的增加和触发适应机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信